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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Vet
Pets & Animals/Pet Medications

Benbow Chemical Packaging, Inc.: Iodine Teat Dips Recalled for Unassured Product Stability

Agency Publication Date: May 2, 2003
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Summary

Benbow Chemical Packaging, Inc. has recalled approximately 1,675 units of ECI Double Dip and ECI Double Dip 2 Iodine Teat Dips across various container sizes, ranging from 1-gallon bottles to 55-gallon drums. This recall was initiated because the manufacturer cannot ensure these products will meet stability specifications or maintain their intended chemical properties throughout their entire shelf life. These products are veterinary medicines used for cattle and were distributed through Eastern Crown, Inc. to customers in New York, Pennsylvania, and Vermont.

Risk

If the products do not meet stability specifications, they may not maintain the correct concentration of iodine, which could lead to ineffective sanitization of animal teats and potentially compromise animal health. No specific animal injuries or incidents have been reported to date.

What You Should Do

  1. Check your supply for ECI DOUBLE DIP Iodine Teat Dip (0.80% iodine) with NDC 060357-0920 or ECI DOUBLE DIP 2 Iodine Teat Dip (0.60% iodine) with NDC 060357-0921.
  2. Identify your specific container size, as the recall affects 1-gallon, 5-gallon, 15-gallon, and 55-gallon containers sold under the Eastern Crown Inc. label.
  3. Immediately stop using the affected teat dip products to ensure the health and safety of your livestock.
  4. Contact your healthcare provider or veterinarian for guidance regarding any animals that may have been treated with these products.
  5. Return any unused product to the place of purchase for a refund or contact the distributor, Eastern Crown Inc., at 877-829-3505 for further instructions.
  6. For additional questions, you may contact the FDA Consumer Complaint Coordinator for your region or the general FDA hotline at 1-888-463-6332.

Your Remedy Options

๐Ÿ’ฐFull Refund

Veterinary drug return and refund protocol.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund.

Affected Products

Product: ECI DOUBLE DIP Iodine Teat Dip, 0.80% iodine (1 gallon)
Model:
NDC 060357-0920
V-170-3
Product: ECI DOUBLE DIP Iodine Teat Dip, 0.80% iodine (5 gallon)
Model:
NDC 060357-0920
V-170-3
Product: ECI DOUBLE DIP Iodine Teat Dip, 0.80% iodine (15 gallon)
Model:
NDC 060357-0920
V-170-3
Product: ECI DOUBLE DIP Iodine Teat Dip, 0.80% iodine (55 gallon drum)
Model:
NDC 060357-0920
V-170-3
Product: ECI DOUBLE DIP 2 Iodine Teat Dip, 0.60% iodine (1 gallon)
Model:
NDC 060357-0921
V-169-3
Product: ECI DOUBLE DIP 2 Iodine Teat Dip, 0.60% iodine (5 gallon)
Model:
NDC 060357-0921
V-169-3
Product: ECI DOUBLE DIP 2 Iodine Teat Dip, 0.60% iodine (15 gallon)
Model:
NDC 060357-0921
V-169-3
Product: ECI DOUBLE DIP 2 Iodine Teat Dip, 0.60% iodine (55 gallon drum)
Model:
NDC 060357-0921
V-169-3

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 25948
Status: Resolved
Manufacturer: Benbow Chemical Packaging, Inc.
Sold By: Eastern Crown, Inc.
Manufactured In: United States
Units Affected: 2 products (1,285 x 1-gallon; 209 x 5-gallon; 63 x 15-gallon; 12 x 55-gallon; 390 x 1-gallon; 48 x 5-gallon; 18 x 15-gallon; 26 x 55-gallon)
Distributed To: New York, Pennsylvania, Vermont

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response